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Lymphocyte Fate and Metabolism: A Clonal Balancing Act.
Nish, Simone A; Lin, Wen-Hsuan W; Reiner, Steven L.
Afiliação
  • Nish SA; Department of Microbiology and Immunology, and Department of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
  • Lin WW; Department of Microbiology and Immunology, and Department of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
  • Reiner SL; Department of Microbiology and Immunology, and Department of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA. Electronic address: sr2978@cumc.columbia.edu.
Trends Cell Biol ; 27(12): 946-954, 2017 12.
Article em En | MEDLINE | ID: mdl-28818395
ABSTRACT
Activated lymphocytes perform a clonal balancing act, yielding a daughter cell that differentiates owing to intense PI3K signaling, alongside a self-renewing sibling cell with blunted anabolic signaling. Divergent cellular anabolism versus catabolism is emerging as a feature of several developmental and regenerative paradigms. Metabolism can dictate cell fate, in part, because lineage-specific regulators are embedded in the circuitry of conserved metabolic switches. Unequal transmission of PI3K signaling during regenerative divisions is reminiscent of compartmentalized PI3K activity during directed motility or polarized information flow in non-dividing cells. The diverse roles of PI3K pathways in membrane traffic, cell polarity, metabolism, and gene expression may have converged to instruct sibling cell feast and famine, thereby enabling clonal differentiation alongside self-renewal.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos / Diferenciação Celular / Polaridade Celular / Linhagem da Célula Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos / Diferenciação Celular / Polaridade Celular / Linhagem da Célula Idioma: En Ano de publicação: 2017 Tipo de documento: Article